Rat Cluster of differentiation 30, CD30 ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
CD30, CD30 antigen,TNFRSF8,D1S166E ,lymphocyte activation antigen CD30; cytokine receptor CD30; D1S166E; Ki-1; CD30L receptor; Ki-1 antigen; tumor necrosis factor receptor superfamily member 8; tumor necrosis factor receptor superfamily, member 8
Search name
Rat CD30 ELISA KIT , Rat CD30 antigen ELISA KIT ,Rat TNFRSF8 ELISA KIT ,Rat D1S166E ELISA KIT ,Rat lymphocyte activation antigen CD30 ELISA KIT ,Rat cytokine receptor CD30 ELISA KIT ,Rat D1S166E ELISA KIT ,Rat Ki-1 ELISA KIT ,Rat CD30L receptor ELISA KIT ,Rat Ki-1 antigen ELISA KIT ,Rat tumor necrosis factor receptor superfamily member 8 ELISA KIT ,Rat tumor necrosis factor receptor superfamily member 8 ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of rat Tumor necrosis factor receptor superfamily member 8 concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Test principle
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Tumor necrosis factor receptor superfamily member 8. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for Tumor necrosis factor receptor superfamily member 8 and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Tumor necrosis factor receptor superfamily member 8, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of Tumor necrosis factor receptor superfamily member 8 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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